Associated Papers
Inherited defects of thyroxine-binding proteins.
Pappa T et al.
Best Practice & Research. Clinical Endocrinology & Metabolism, 2015
A novel EBP c.224T>A mutation supports the existence of a male-specific disorder independent of CDPX2.
Barboza-Cerda MC et al.
American Journal of Medical Genetics. Part A, 2014
The role of the abnormalities in the distal pathway of cholesterol biosynthesis in the Conradi-Hünermann-Happle syndrome.
Cañueto J et al.
Biochimica Et Biophysica Acta, 2014
TM6SF2 and MAC30, new enzyme homologs in sterol metabolism and common metabolic disease.
Sanchez-Pulido L et al.
Frontiers in Genetics, 2014
Clinical, molecular and biochemical characterization of nine Spanish families with Conradi-Hünermann-Happle syndrome: new insights into X-linked dominant chondrodysplasia punctata with a comprehensive review of the literature.
Cañueto J et al.
The British Journal of Dermatology, 2012
PTGDR gene in asthma: a functional, genetic, and epigenetic study.
Isidoro-García M et al.
Allergy, 2011
Promoter genetic variants of prostanoid DP receptor (PTGDR) gene in patients with asthma.
Sanz C et al.
Allergy, 2006
Novel mutations in X-linked dominant chondrodysplasia punctata (CDPX2).
Whittock NV et al.
The Journal of Investigative Dermatology, 2003
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